ID: 7532 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76326799..76358991, complement) | 14-3-3GAMMA, DEE56, EIEE56, PPP1R170 | 605356 |
ID: 90780 | pygopus family PHD finger 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154957026..154961782, complement) | 1190004M21Rik | 606903 |
ID: 221710 | small integral membrane protein 13 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (11093834..11138733) | C6orf228 | |
ID: 64326 | COP1 E3 ubiquitin ligase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (175944831..176207286, complement) | CFAP78, FAP78, RFWD2, RNF200 | 608067 |
ID: 533 | ATPase H+ transporting V0 subunit b [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974960..43978295) | ATP6F, HATPL, VMA16 | 603717 |
ID: 9986 | Ras converting CAAX endopeptidase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66843441..66846552) | FACE2A, RCE1B, RCE1 | 605385 |
ID: 11335 | chromobox 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (26201443..26213607) | HECH, HP1-GAMMA, HP1Hs-gamma, HP1gamma | 604477 |
ID: 253260 | RPTOR independent companion of MTOR complex 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (38937920..39074399, complement) | AVO3, PIA, hAVO3 | 609022 |
ID: 8976 | WASP like actin nucleation promoting factor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (123681943..123749003, complement) | N-WASP, NWASP, WASPB | 605056 |
ID: 8566 | pyridoxal kinase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43719129..43762299) | C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK, PRED79 | 179020 |
ID: 6738 | Ro60, Y RNA binding protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (193059612..193091777) | RORNP, SSA2, TROVE2 | 600063 |
ID: 5834 | glycogen phosphorylase B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25248085..25298012) | GPBB | 138550 |
ID: 64839 | F-box and leucine rich repeat protein 17 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (107859035..108382098, complement) | FBXO13, Fbl17, Fbx13 | 609083 |
ID: 51306 | family with sequence similarity 13 member B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (137937960..138052178, complement) | ARHGAP49, C5orf51, KHCHP, N61, FAM13B | 609371 |
ID: 103910 | myosin light chain 12B [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (3262133..3278461) | MLC-B, MRLC2 | 609211 |
ID: 23358 | ubiquitin specific peptidase 24 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (55066359..55215364, complement) | | 610569 |
ID: 7733 | zinc finger protein 180 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44474431..44500522, complement) | HHZ168 | 606740 |
ID: 23052 | endonuclease domain containing 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (95089846..95132645) | | 619568 |
ID: 64968 | mitochondrial ribosomal protein S6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073578..34143030) | C21orf101, MRP-S6, RPMS6, S6mt, bS6m | 611973 |
ID: 22828 | SR-related CTD associated factor 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (154733378..154834244) | RBM16 | 616024 |